SCHEMBL506568

SCHEMBL506568

COc1cccc(C=O)n1

nearest known ligand 0.47

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
IDH1 O75874 1/20 0.47
TERT O14746 3/20 0.45
BTK Q06187 1/20 0.45
ALDH1A1 P00352 2/20 0.41
TGFBR1 P36897 2/20 0.40
CCR1 P32246 1/20 0.40
NFE2L2 Q16236 2/20 0.38
MAPT P10636 1/20 0.38
ALOX5 P09917 1/20 0.37
DDB1 Q16531 1/20 0.36
CRBN Q96SW2 1/20 0.36
TLR2 O60603 1/20 0.36
ERN1 O75460 1/20 0.36
TLR1 Q15399 1/20 0.36
TLR6 Q9Y2C9 1/20 0.36
CA1 P00915 1/20 0.36
CA2 P00918 1/20 0.36

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL29432664 1.00 IDH1 (0.47) IDH1TERTBTKALDH1A1TGFBR1
SCHEMBL16180241 0.89 BTK (0.55) IDH1TERTBTKALDH1A1TGFBR1
SCHEMBL10988595 0.82 TERT (0.52) TERTALDH1A1NFE2L2MAPT
SCHEMBL1984412 0.81 IDH1 (0.44) IDH1BTKALDH1A1TGFBR1NFE2L2
SCHEMBL11383636 0.79 TERT (0.51) TERTALDH1A1NFE2L2MAPT
SCHEMBL931475 0.79 IDH1 (0.43) IDH1BTKALDH1A1TGFBR1NFE2L2
SCHEMBL18901393 0.79 IDH1 (0.43) IDH1BTKALDH1A1TGFBR1NFE2L2
SCHEMBL3081313 0.79 IDH1 (0.47) IDH1BTKALDH1A1TGFBR1NFE2L2
SCHEMBL31621100 0.79 IDH1 (0.43) IDH1BTKALDH1A1TGFBR1NFE2L2
SCHEMBL28873288 0.79 IDH1 (0.43) IDH1BTKALDH1A1TGFBR1NFE2L2

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 578 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119039275-A Preparation method of biologically active imidazole derivative 2,3, 5-tripyridine substituted imidazole 武汉理工大学深圳研究院 2024-11-29 CN claimed
EP-4452263-A1 COMBINATION OF A TASK1/3 CHANNEL BLOCKER WITH A P2X3 RECEPTOR ANTAGONIST FOR THE TREATMENT OF SLEEP APNEA Bayer Aktiengesellschaft (DE) 2024-10-30 EP claimed
CN-116947754-A Antitumor compound, antitumor drug, preparation method and application 北京中医药大学 2023-10-27 CN claimed
WO-2023118122-A1 COMBINATION OF A TASK1/3 CHANNEL BLOCKER WITH A P2X3 RECEPTOR ANTAGONIST FOR THE TREATMENT OF SLEEP APNEA BAYER AKTIENGESELLSCHAFT (DE) 2023-06-29 WO claimed
WO-2023118126-A1 COMBINATION OF A TASK1/3 CHANNEL BLOCKER WITH A NOREPINEPHRINE REUPTAKE INHIBITOR FOR THE TREATMENT OF SLEEP APNEA BAYER AKTIENGESELLSCHAFT (DE) 2023-06-29 WO claimed
CN-116057057-A Conjugates of alpha 2-adrenoceptor subtype C (alpha-2C) antagonists and TASK1/3 channel blockers for the treatment of sleep apnea 拜耳公司 2023-05-02 CN claimed
EP-3886806-A1 PROCESS FOR PRODUCING PHARMACEUTICAL DOSAGE FORMS CONTAINING TASK-1 AND TASK-3 CHANNEL INHIBITORS, AND THE USE OF SAME IN BREATHING DISORDER THERAPY Bayer Aktiengesellschaft (DE) 2021-10-06 EP claimed
CN-113194924-A Method for preparing pharmaceutical dosage forms comprising inhibitors of the TASK-1 and TASK-3 channels and their use in the treatment of respiratory disorders 拜耳公司 2021-07-30 CN claimed
EP-3558380-A1 PHARMACEUTICAL DOSAGE FORMS CONTAINING TASK-1 AND TASK-3 CHANNEL INHIBITORS, AND THE USE OF SAME IN BREATHING DISORDER THERAPY Bayer Pharma Aktiengesellschaft (DE) 2019-10-30 EP claimed
EP-3558379-A1 PHARMACEUTICAL DOSAGE FORMS CONTAINING TASK-1 AND TASK-3 CHANNEL INHIBITORS, AND THE USE OF SAME IN BREATHING DISORDER THERAPY Bayer Pharma Aktiengesellschaft (DE) 2019-10-30 EP claimed
CN-103923110-B There is the preparation method of the benzimidizole derivatives metal complexes of anti-microbial activity HARBIN INSTITUTE OF TECHNOLOGY (CN) 2016-03-16 CN claimed
CN-102603776-B A kind of preparation method of luminous organic material 2-(benzimidazolyl-)-6-methoxv-pyridine Zn complex HARBIN INSTITUTE OF TECHNOLOGY (CN) 2015-08-19 CN claimed
WO-2013049164-A1 SUBSTITUTED OCTAHYDROPYRROLO[1,2-a]PYRAZINES AS CALCIUM CHANNEL BLOCKERS ABBVIE INC. (US) 2013-04-04 WO claimed
US-12577247-B2 Diaminopyrazolo[1,5-a]pyrimidine-6-carbonitrile compounds as adenosine 2A receptor and adenosine 2B receptor antagonist Bugworks Research, Inc. (US) 2026-03-17 US disclosed
EP-4703361-A1 PYRIDAZINONE TRPC4/5 INHIBITOR AND USE THEREOF Shanghai Institute of Materia Medica, Chinese Academy of Sciences (CN) 2026-03-04 EP disclosed
EP-4698524-A1 TRIARYL AGONISTS OF ALPHA-2 ADRENERGIC RECEPTORS Alceptor Therapeutics, Inc. (US) 2026-02-25 EP disclosed
EP-0863141-A1 SUBSTITUTED HETEROAROMATIC DERIVATIVES BANYU PHARMACEUTICAL CO., LTD. (JP) 1998-09-09 EP disclosed
EP-0656359-A1 Substituted 6,11-ethano-6,11-dihydrobenzo[b]quinolizinium salts and compositionsand methods of use thereof STERLING WINTHROP INC. (US) 1995-06-07 EP disclosed
EP-0196232-B1 PLATING BATH AND METHOD FOR ELECTROPLATING TIN AND/OR LEAD MCGEAN-ROHCO, INC. (US) 1991-11-21 EP disclosed
EP-0196232-A2 Plating bath and method for electroplating tin and/or lead MCGEAN-ROHCO, INC. (US) 1986-10-01 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-12577247-B2 Diaminopyrazolo[1,5-a]pyrimidine-6-carbonitrile compounds as adenosine 2A receptor and adenosine 2B receptor antagonist ADORA1, ADORA3, ADORA2A IDH1 1583/4885TERT 2747/4885BTK 2448/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.